Results From a Mexican Acute Promyelocytic Leukemia.

NCT ID: NCT04562818

Last Updated: 2020-09-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

360 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-01-01

Study Completion Date

2018-01-01

Brief Summary

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Retrospective, observational study, comparing treatments of acute promyelocytic leukemia in different centers in México.

There is no sufficient information about acute promyelocytic leukemia in America Latina, particularly in Mexico.

For these reason the investigators started a study adding all promyelocityc patients from the main Hospital in Mexico in order to put together a group of patient and analyze the response, overall survival and what are the characteristics of the population.

The investigators included 5 Hospital in Mexico City and states as Monterrey, Guadalajara, San Luis Potosi, Puebla, Veracruz, Yucatán, Oaxaca, Guanajuato, Estado de México.

Even do, the investigators didn´t have arsenic trioxide they are treating patients with standard chemotherapy. These paper will help to show the authorities that the cost of treating patient with standard chemotherapy is much more higher than ATO-ATRA. The investigators are now doing a cost benefit analysis so the investigators, can soon have ATO treatment as standard of care in Mexico for the treatment of acute promyelocytic leukemia.

Detailed Description

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A multicentric, retrospective, descriptive, longitudinal study was carried out. Between January 2007 and January 2017, patients of both sexes and different ages, who were candidates for receiving intensive chemotherapy along with tretinoin were included in the study. The diagnosis for Acute Promyelocytic Leukemia was determined based on the following criteria: abnormal promyelocytes in the bone marrow and verification of the t(15;17) translocation by karyotype or using RT-PCR to determine the genetic lesion and define the type of PML/RARA isoform.

In Mexico the investigators still treating patients with anthracycline and cytarabine + transretinoic acid. These information will help the authorities to realize the importance of having arsenic trioxide as part of the treatment of these disease, knowing the amount of patient that the investigators have in Mexico, knowing that in the hispanic race the incidence is greater.

Conditions

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Promyelocytic Leukemia, Acute

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

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Daunorrubicin

Patient treated with daunorrubicin

Diagnosis

Intervention Type DIAGNOSTIC_TEST

Determine the number of center that are able to process PCR or FISH/Karyotype for PML/RAR or t(15;17)

Molecular and Karyotype

Intervention Type DIAGNOSTIC_TEST

To realize the need of having more center we the technology to perform all of these tests

Leucocytes

Intervention Type DIAGNOSTIC_TEST

Idarrubicin

Patient treated with idarrubicin

Diagnosis

Intervention Type DIAGNOSTIC_TEST

Determine the number of center that are able to process PCR or FISH/Karyotype for PML/RAR or t(15;17)

Molecular and Karyotype

Intervention Type DIAGNOSTIC_TEST

To realize the need of having more center we the technology to perform all of these tests

Leucocytes

Intervention Type DIAGNOSTIC_TEST

Interventions

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Diagnosis

Determine the number of center that are able to process PCR or FISH/Karyotype for PML/RAR or t(15;17)

Intervention Type DIAGNOSTIC_TEST

Molecular and Karyotype

To realize the need of having more center we the technology to perform all of these tests

Intervention Type DIAGNOSTIC_TEST

Leucocytes

Intervention Type DIAGNOSTIC_TEST

Other Intervention Names

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FISH Karyotype PCR Risk status

Eligibility Criteria

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Inclusion Criteria

* Actute Promyelocytic leukemia PML/RAR alfa + Diabetes mellitus Hypertension Asthma Chronic renal disease

Exclusion Criteria

* Non Acute Promyelocytic leukemia Younger than 15 years old
Minimum Eligible Age

15 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Instituto Nacional de Cancerologia de Mexico

OTHER

Sponsor Role lead

Responsible Party

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Nidia Paulina Zapata-Canto

Assistant Professor of Hematology Department (Acute Myeloid Leukemia)

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Nidia Zapata

Mexico City, Mexico City, Mexico

Site Status

Countries

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Mexico

References

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Reference Type RESULT
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Reference Type RESULT
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Reference Type RESULT
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Other Identifiers

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INCancerologiaMexico

Identifier Type: -

Identifier Source: org_study_id

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